Professional Documents
Culture Documents
CME
CNE
Blackwell Futura Media Services is accredited by the Accreditation Council for Continuing Medical Education to provide continuing medical education (CME)
for physicians.
Blackwell Futura Media Services designates this journal-based CME for a maximum of 1 AMA PRA Category 1 Credit. Physicians should only claim credit
commensurate with the extent of their participation in the activity.
The American Cancer Society (ACS) is accredited as a provider of continuing nursing education (CNE) by the American Nurses Credentialing Centers Commission
on Accreditation.
Accredited status does not imply endorsement by the ACS or the American Nurses Credentialing Center of any commercial products displayed or discussed in
conjunction with an educational activity. The American Cancer Society gratefully acknowledges the sponsorship provided by Wiley-Blackwell for hosting these
CNE activities.
EDUCATIONAL OBJECTIVES:
After reading the article Nutrition and Physical Activity Guidelines for Cancer Survivors, the learner should be able to provide advice to patients regarding current
evidence relevant to the impact of nutrition and physical activity choices on:
1. Symptom management in patients undergoing cancer therapy.
2. Cancer recurrence, survival, and risk of other chronic diseases (including second primary cancers) after the treatment of cancer.
ACTIVITY DISCLOSURES
No commercial support has been accepted related to the development or publication of this activity.
AUTHOR DISCLOSURES
Cheryl L. Rock, PhD, RD; Colleen Doyle, MS, RD; Wendy Demark-Wahnefried, PhD, RD; Jeffrey Meyerhardt, MD, MPH; Kerry S. Courneya, PhD;
Anna L. Schwartz, FNP, PhD, FAAN; Elisa V. Bandera, MD, PhD; Kathryn K. Hamilton, MA, RD, CSO, CDN; Barbara Grant, MS, RD, CSO, LD;
Marji McCullough, ScD, RD; Tim Byers, MD, MPH; Ted Gansler, MD, MBA, MPH, have no conicts of interest to disclose.
This activity has been reviewed and revised on the basis of feedback provided by the American Cancer Society 2011 Nutrition, Physical Activity and
Cancer Survivorship Advisory Committee. The committee had no conicts of interest to disclose.
Conicts of interest have been identied and resolved in accordance with Blackwell Futura Media Services Policy on Activity Disclosure and Conict of Interest.
SCORING
A score of 70% or better is needed to pass a quiz containing 10 questions (7 correct answers), or 80% or better for 5 questions (4 correct answers).
CME INSTRUCTIONS ON RECEIVING CME CREDIT
This activity is intended for physicians. For information concerning the applicability and acceptance of CME credit for this activity, please consult your
professional licensing board.
This activity is designed to be completed within 1 hour; physicians should claim only those credits that reect the time actually spent in the activity. To
successfully earn credit, participants must complete the activity during the valid credit period, which is up to 2 years from the time of initial publication.
CNE INSTRUCTIONS ON RECEIVING CNE CONTACT HOURS
This activity is intended for nurses. For information on applicability and acceptance of continuing education credit for this activity, please consult your
professional licensing board.
This activity is designed to be completed within 1.5 hours; nurses should claim only those credits that reect the time actually spent in the activity. To
successfully earn credit, participants must complete the activity during the valid credit period, which is up to 2 years from initial publication.
Log on to acsjournals.com/ce
Read the target audience, educational objectives, and activity disclosures.
Read the activity contents in print or online format.
Reect on the activity contents.
Access the examination, and choose the best answer to each question.
Complete the required evaluation component of the activity.
Claim your certicate.
This activity will be available for CME/CNE credit for 1 year following its launch date. At that time, it will be reviewed and potentially updated and
extended for an additional 12 months.
All CME/CNE quizzes are offered online FREE OF CHARGE. Please log in at acsjournals.com/ce. New users can register for a FREE account. Registration
will allow you to track your past and ongoing activities. After successfully completing each quiz, you may instantly print a certicate, and your online record of
completed courses will be updated automatically.
242
Cancer survivors are often highly motivated to seek information about food choices, physical activity, and dietary supplements to
improve their treatment outcomes, quality of life, and overall survival. To address these concerns, the American Cancer Society
(ACS) convened a group of experts in nutrition, physical activity, and cancer survivorship to evaluate the scientific evidence and
best clinical practices related to optimal nutrition and physical activity after the diagnosis of cancer. This report summarizes their
findings and is intended to present health care providers with the best possible information with which to help cancer survivors
and their families make informed choices related to nutrition and physical activity. The report discusses nutrition and physical activity guidelines during the continuum of cancer care, briefly highlighting important issues during cancer treatment and for patients
with advanced cancer, but focusing largely on the needs of the population of individuals who are disease free or who have stable
disease following their recovery from treatment. It also discusses select nutrition and physical activity issues such as body weight,
food choices, food safety, and dietary supplements; issues related to selected cancer sites; and common questions about diet,
physical activity, and cancer survivorship. CA Cancer J Clin 2012;62:242-274. VC 2012 American Cancer Society.
To earn free CME credit or nursing contact hours for successfully completing the online quiz based on this article, go to
acsjournals.com/ce.
Introduction
A cancer survivor is defined as anyone who has been diagnosed with cancer, from the time of diagnosis through the rest of
their life.1 Given advances in early detection and treatment, the number of US cancer survivors is estimated to exceed 12
million and is growing steadily, so that approximately one in every 25 Americans is now a cancer survivor.1,2 Many cancer
survivors are highly motivated to seek information about food choices, physical activity, dietary supplement use, and
complementary nutritional therapies to improve their response to treatment, speed recovery, reduce their risk of recurrence,
and improve their quality of life.3
The trajectory of cancer survivorship is marked by 3 general phases: 1) active treatment and recovery; 2) living after
recovery, including survivors who are disease free or who have stable disease; and 3) advanced cancer and end of life.
Approximately 68% of Americans diagnosed with cancer now live more than 5 years,4 and their nutritional needs change
over the course of survivorship. The need for informed lifestyle choices for cancer survivors becomes particularly important
as they look forward to the successful completion of therapy and seek self-care strategies to improve their long-term outcomes. For many long-term cancer survivors, healthy weight management, a healthful diet, and a physically active lifestyle
aimed at preventing recurrence, second primary cancers, and other chronic diseases should be a priority. For other survivors,
regaining health following a difficult treatment or managing nutritional needs and activity levels while living with advanced
cancer becomes a particular challenge.
1
Professor, Department of Family and Preventive Medicine, School of Medicine, University of California, San Diego, La Jolla, CA; 2Director, Nutrition and
Physical Activity, Cancer Control Science, American Cancer Society, Atlanta, GA; 3Professor and Webb Endowed Chair of Nutrition Sciences, University of
Alabama at Birmingham, Birmingham, AL; 4Associate Professor of Medicine, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA; 5Professor
and Canada Research Chair in Physical Activity and Cancer, University of Alberta, Edmonton, Alberta, Canada; 6Affiliate Professor, University of Washington,
Seattle, WA, Associate Professor, Idaho State University, Pocatello, ID; 7Associate Professor, Department of Epidemiology, The Cancer Institute of New
Jersey, New Brunswick, NJ; 8Outpatient Oncology Dietitian, Carol G. Simon Cancer Center, Morristown Memorial Hospital, Morristown, NJ; 9Oncology
Nutritionist, Saint Alphonsus Regional Medical Center Cancer Care Center, Boise, ID; 10Nutritional Epidemiologist, Epidemiology and Surveillance Research,
American Cancer Society, Atlanta, GA; 11Associate Dean for Public Health Practice, Colorado School of Public Health, Associate Director for Cancer
Prevention and Control, University of Colorado Cancer Center, Aurora, CO; 12Director, Medical Content, American Cancer Society, Atlanta, GA.
Corresponding author: Colleen Doyle, MS, RD, American Cancer Society, 250 Williams St NW, Suite 600, Atlanta, GA 30303; colleen.doyle@cancer.org
DISCLOSURES: The authors report no conflicts of interest.
C
V
243
Survivors should ask their health care provider for a referral to see an RD, preferably an RD who is also a CSO, if they experience nutrition-related challenges.
If an oncology dietitian is not available in the medical or surgical practice or medical center where they receive their cancer treatment and care, an
appointment with a dietitian associated with their primary care provider clinic may be arranged.
Survivors, caregivers, and providers can also consult the Academy of Nutrition and Dietetics to identify a private practice dietitian in their area.
RD indicates registered dietitian; CSO certified specialist in oncology.
245
Achieve a dietary pattern that is high in vegetables, fruits, and whole grains.
l Follow the American Cancer Society Guidelines on Nutrition and Physical
Activity for Cancer Prevention.
247
19
20
21
22
23
24
25
HEIGHT
0
26
27
28
29
30
31
32
33
34
35
WEIGHT IN POUNDS
00
4 10
91
96
100
105
110
115
119
124
129
134
138
143
148
153
158
162
167
40 1100
94
99
104
109
114
119
124
128
133
138
143
148
153
158
163
168
173
97
102
107
112
118
123
128
133
138
143
148
153
158
163
168
174
179
0 00
100
106
111
116
122
127
132
137
143
148
153
158
164
169
174
180
185
0 00
104
109
115
120
126
131
136
142
147
153
158
164
169
175
180
186
191
0 00
53
107
113
118
124
130
135
141
146
152
158
163
169
175
180
186
191
197
50 400
110
116
122
128
134
140
145
151
157
163
169
174
180
186
192
197
204
0 00
114
120
126
132
138
144
150
156
162
168
174
180
186
192
198
204
210
0 00
118
124
130
136
142
148
155
161
167
173
179
186
192
198
204
210
216
0 00
121
127
134
140
146
153
159
166
172
178
185
191
198
204
211
217
223
0 00
58
125
131
138
144
151
158
164
171
177
184
190
197
203
210
216
223
230
50 900
128
135
142
149
155
162
169
176
182
189
196
203
209
216
223
230
236
51
52
55
56
57
00
132
139
146
153
160
167
174
181
188
195
202
209
216
222
229
236
243
00
5 10
5 11
136
143
150
157
165
172
179
186
193
200
208
215
222
229
236
243
250
140
147
154
162
169
177
184
191
199
206
213
221
228
235
242
250
258
0 00
61
144
151
159
166
174
182
189
197
204
212
219
227
235
242
250
257
265
60 200
148
155
163
171
179
186
194
202
210
218
225
233
241
249
256
264
272
0 00
152
160
168
176
184
192
200
208
216
224
232
240
248
256
264
272
279
63
HEALTHY WEIGHT
OVERWEIGHT
OBESE
249
Diet Composition
Protein, carbohydrate, and fat all contribute energy to the
diet, and each of these dietary constituents is available from
a wide variety of foods. Because many cancer survivors are
at high risk of other chronic diseases, such as heart disease,
the recommended amounts and types of fat, protein, and
carbohydrate to reduce cardiovascular disease risk are also
appropriate for cancer survivors, particularly if they are at or
above their recommended body weight.46,47,49,52
The Institute of Medicine and current Federal Guidelines,
as well as the American Heart Association (AHA), recommend a spectrum of dietary composition for the adult
population: fat: 20% to 35% of energy (AHA: 25%-35%),
carbohydrate: 45% to 65% of energy (AHA: 50%-60%); and
protein: 10% to 35% of energy (at least 0.8 g/kg).46,49,124
Several studies have examined the relationship between
fat intake and survival after the diagnosis of breast
cancer; evidence from these observational studies is mixed.
Aerobic dance
Biking faster than 10 miles per hour
Fast dancing
Heavy gardening (digging, hoeing)
Hiking uphill
Jumping rope
Martial arts (such as karate)
Race walking, jogging, or running
Sports with a lot of running (basketball, hockey, soccer)
Swimming fast or swimming laps
Tennis (singles)
251
Dietary Supplements
According to the Dietary Supplement Health and Education
Act (DSHEA) of 1994, dietary supplements include vitamins;
minerals; herbs/botanicals; amino acids; and a concentrate,
metabolite, constituent extract, or combination of any of
253
254
Alcohol
Food Safety
255
there remains a need for a randomized controlled trial to further test the benefit of exercising in preventing cancer recurrence and improving survival in women with breast cancer.62
Even with the increased use of sentinel lymph node
dissection, lymphedema remains a concern among breast
cancer survivors. However, aerobic physical activity and
resistance training appear to be both safe and effective in
reducing the incidence of lymphedema among survivors at
high risk of this condition, and in improving the symptoms
and severity of lymphedema for those in whom the condition
was preexisting.111,112 Progressive resistance training under
the supervision of a trained exercise therapist and using
appropriate compression garments is recommended. In addition, because obesity is a major risk factor for lymphedema,
weight loss is recommended among survivors who are
overweight or obese.
Research is currently under way to evaluate various
components of dietary patterns on cancer-specific outcomes,
as well as overall health. An observational study found that
dietary pattern was important for overall survival among
breast cancer survivors, with those who ate a Western diet
having poorer overall survival and those who ate a dietary
pattern characterized by high amounts of fruits, vegetables,
and whole grains having better overall survival; however,
neither dietary pattern was associated with breast cancer
recurrence specifically.120 One factor that tends to separate
these 2 dietary patterns is fat; however, to date, evidence
that dietary fat intake could be associated with risk of
recurrence or survival is not strongly or consistently
supported, especially when total energy intake and the
degree of obesity are considered.202,203
Two large clinical trials tested whether change in diet
composition can reduce the risk of recurrence and increase
overall survival in women who have been diagnosed with
breast cancer. While the WINS low-fat dietary intervention group exhibited a borderline significant 24% reduction
in risk of recurrence, the group also lost weight, so it is
possible that the benefits were due to weight loss and not a
reduction in fat intake. In the WHEL Study, a reduction
in dietary fat was among the dietary goals, and an effect of
the diet intervention (which was not associated with weight
loss) was not observed.
Eating more vegetables is inconsistently related to reducing
breast cancer risk, and the evidence that fruit intake is related
to recurrence or survival is weak.204,205 In the WHEL Study,
the major intervention was increased vegetable and fruit
intake, although women in the intervention group were also
encouraged to reduce their fat and increase their fiber
intakes.206 Recurrence-free survival did not differ between
the 2 study arms in that study,122 although the fruit and
vegetable intake of these women was already high, averaging
greater than 7 servings per day at the beginning of the study.
256
Colorectal Cancer
Epidemiologic, clinical, and laboratory research indicates
that diet, adiposity, and physical activity have a significant
influence on the risk of developing colorectal cancer.213,214
Over the past decade, there has been an increasing number
of studies that have examined the influence of these modifiable host factors on physical well-being, quality of life, and
cancer recurrences and survival.78
Several observational studies have shown that higher
physical activity levels or meeting physical activity guidelines
is associated with better patient-reported quality of life,
physical functioning, and fatigue.215-220 One randomized
trial of an exercise intervention in colorectal cancer survivors
demonstrated that participants whose aerobic fitness
increased over the course of the intervention, regardless of
group assignment, reported significantly improved quality
of life, physical functioning, and psychosocial distress
compared with participants whose fitness decreased.221
Recently emerging, prospective, observational data have
shown that colorectal cancer survivors who are physically
active lower their risk of cancer recurrence, colorectal
cancer-specific mortality, and/or overall mortality.104-107,222
These data have led to the initiation of the Colon Health
and Life-Long Exercise Change (CHALLENGE) trial,
257
Endometrial Cancer
Endometrial cancer is the most common gynecologic cancer
and the fourth most common cancer in women.4 The
prognosis of endometrial cancer is related to the stage of
disease at diagnosis, with a 90% survival rate if diagnosed at
stage I,232 which is common because the main symptom,
abnormal bleeding, is easy to detect and likely to cause
women to seek medical attention.
Obesity is a strong risk factor for the development of
endometrial cancer. Approximately 70% to 90% of women
with type 1 endometrial cancer (the most common type) are
obese.233 However, there are few studies of the role of
obesity in endometrial cancer prognosis. Prediagnosis
obesity has been shown to be associated with a significant
increase in endometrial cancer mortality.234 This may be
related to common comorbidities among obese women,
such as type 2 diabetes and hypertension, which may
complicate cancer treatment.76 In a study using data from
participants in a Gynecologic Oncology Group trial of early
stage endometrial cancer, obesity was associated with
higher mortality from causes other than endometrial cancer
but not with recurrence.235 Obese women tend to develop
less aggressive endometrial cancer236-238; however, decreased
overall survival among obese endometrial cancer patients has
been seen in some studies,235,239 but not in others.236-238
No studies have reported on the role of dietary factors
and physical activity in the prognosis of endometrial
cancer. Although the role of obesity in endometrial cancer
prognosis is not completely understood, studies have shown
that a higher BMI and a sedentary lifestyle are associated
with a poorer quality of life among endometrial cancer
survivors.233,240,241
Ovarian Cancer
Ovarian cancer is the leading cause of death from gynecologic
malignancies in the United States.4 Symptoms tend be
nonspecific, making early detection difficult. Consequently,
most ovarian cancers are diagnosed at an advanced stage
when the prognosis is poor, with an overall 10-year survival
rate of 39%.4 The role of lifestyle factors in ovarian cancer
prognosis is largely unknown.138,242 To our knowledge, only
3 studies139,140,243 have evaluated the role of dietary factors
in ovarian cancer survival. These 3 studies were based on prospective follow-up of the cases participating in case-control
studies and evaluated the association between prediagnosis
dietary intake and mortality outcomes. One study, conducted
in China, focused on the role of green tea and reported that a
higher frequency and quantity of green tea intake after
258
Lung Cancer
Lung cancer treatment is often aggressive and causes
adverse effects. Furthermore, many lung cancer survivors
are underweight and have low blood nutrient levels
even before diagnosis as a result of the adverse effects of
inadequate diets, smoking, or both on micronutrient status.
During treatment and the immediate recovery period, lung
cancer survivors may benefit from eating foods that are
energy-dense and easy to swallow. Small, frequent meals
may be easier to manage than 3 large meals per day.
Medications and nutritional support via energy-dense nutritional supplements or enteral nutrition may be helpful for
those experiencing weight loss.257 If nutrient deficiencies are
present or survivors cannot eat enough to adequately meet
micronutrient needs, a multivitamin-mineral supplement is
advisable, either in pill or liquid form.
Patients with lung cancer present with a complex variety
of symptoms that can limit physical function and lead to
distress, including dyspnea, air hunger, anxiety, muscle
weakness, fatigue, and limited cardiopulmonary function.
Despite these issues, there have been several clinical trials
that have successfully demonstrated the feasibility of
exercise interventions in select lung cancer patients. A
recent systematic review of 16 studies inclusive of 675 lung
cancer patients demonstrated that patients participating in
an exercise intervention prior to surgery reported improvements in exercise capacity but no change in health-related
quality of life immediately after the intervention.258
Furthermore, other studies of exercise following standard
lung cancer treatment demonstrated improvements in
exercise capacity but had conflicting results with respect to
the impact on quality of life. More research is needed in
this cancer patient population.
The possible effect (either beneficial or harmful) of
nutritional supplements other than beta-carotene after the
diagnosis of lung cancer has not been extensively studied.
One clinical trial of selenium and skin cancer noted a
reduced incidence of lung cancer in association with
selenium supplementation.259 While some researchers have
VOLUME 62 _ NUMBER 4 _ JULY/AUGUST 2012
259
Prostate Cancer
Most research on nutrition and prostate cancer has focused
on prostate cancer incidence.266,267 Because asymptomatic
prostate cancer is very common in older men, the same
lifestyle factors that are associated with a reduced prostate
cancer incidence might also reduce the rate of prostate cancer growth after diagnosis, thus preventing or slowing the
progression of early stage prostate cancer. However, notable
exceptions are body weight and obesity, which appear to
be related to cancer progression and the more aggressive
forms of prostate cancer, and not the latent or indolent
disease that appears to be an artifact of aging.268 In recent
years, a few studies have tried to determine directly whether
such dietary factors may prolong survival from prostate
cancer or may influence biomarkers (eg, prostate-specific
antigen [PSA] levels) that are associated with outcomes for
men with prostate cancer.
A high intake of foods from animal sources, especially
foods high in saturated fat, has been associated with an
increased risk of prostate cancer.203,266 Whether this
increased risk is due to saturated fat per se or to the consumption of red meat and high-fat dairy products is
unclear. The observation that fatty fish intake may decrease
prostate cancer mortality rates suggests that, if fat is
important, the type of fat may play a key role. There are 2
follow-up studies of dietary factors and survival in prostate
cancer survivors. One found that saturated fat intake (but
not total fat) is associated with worse survival,269 and the
other found that monounsaturated fat intake is associated
260
261
treatment and the period of time immediately after treatment. Patients are encouraged to eat soft, moist foods
throughout treatment to maintain their swallowing function. Patients with esophageal and gastric cancers may need
support through treatment as well. This population may
require placement of either a gastrostomy tube or a jejunostomy tube, depending on anticipated or performed surgical
interventions. When tube feeding is started immediately after surgery for esophageal or gastric cancer, it may reduce
both the duration of intensive care unit treatment and total
hospital stay.286,287
Several small studies have shown that physical activity
may improve functioning, reduce pain and disability, and be
related to quality of life in head and neck cancer survivors.288-290 One study of 52 head and neck cancer survivors
that compared progressive resistance exercise with standard
physical therapy demonstrated that resistance training significantly improved self-reported shoulder pain and disability,
upper extremity strength, and upper extremity endurance.289
Furthermore, changes in neck dissection impairment, fatigue,
and quality of life nonsignificantly favored those patients
treated with resistance training.
Patients with esophageal or gastric cancer may have
symptoms such as early satiety, dumping syndrome, or
malabsorption that affect food and nutrient intake, as well
as absorption and digestion; the effects of treatment may
result in long-term or permanent nutritional complications.
Survivors with esophageal cancer can experience temporary
or long-term dysphagia, odynophagia, gastroesophageal
reflux, and early satiety.9 Diet modifications determined
with the assistance of an oncology-certified registered
dietitian can help to manage some of these treatmentrelated conditions, help regain or maintain a healthy
weight, and restore some quality of life.
The nutritional management of patients with gastric cancer
is based on determining the portion of the stomach involved
with disease or the condition after surgical resection. If
either the esophageal or pyloric sphincter has been affected,
diet modifications will involve small, more frequent meals/
snacks, no concentrated sweets, and the consumption of
fluids between meals due to early satiety. In addition, the
patient is advised to stop eating 3 hours before bedtime or
going to bed to avoid aspiration. There is a significant risk
of micronutrient deficiencies in this patient population due
to the alteration of the digestion process and absorption of
minerals such as iron and calcium and vitamins such as
vitamin B12. If possible, a patients status should be tested
pretreatment and followed through the treatment and
long-term survivorship period.
In the case of pancreatic cancer, there is increasing
evidence that supplementation with omega-3 fatty
acids has a favorable effect on short-term weight status,
262
Alcohol
Does Alcohol Increase the Risk of Cancer Recurrence?
Many studies have found a link between alcohol intake and
risk of some primary cancers, including cancers of the mouth,
pharynx, larynx, esophagus, liver, breast, and probably colon
cancer.47,170,165 In individuals who have already received a
diagnosis of cancer, alcohol intake could also affect the
risk of new primary cancers of these sites.171 Alcohol intake
can increase the circulating levels of estrogens, which
theoretically could increase the risk of a recurrence of
ER-positive breast cancer; currently, however, only a few
studies have explored alcohol use among breast cancer
survivors, with approximately one-half showing a detrimental
effect and one-half showing benefit or no harm. One study
suggests that the detrimental effects of alcohol may be
exacerbated in women who are overweight or obese.176
Given that alcohol does exert cardioprotective effects, the
question of whether to consume it or not depends heavily
upon hereditary disposition and risk of recurrence versus
risk of cardiovascular disease.
Antioxidants
What Do Antioxidants Have to Do With Cancer?
Antioxidants exist naturally in many forms and help prevent
oxidative damage to tissues. Because oxidative damage may
be important in the development of cancer, it has been
hypothesized that increasing intake of antioxidants from
foods or supplements may help prevent cancer. Some
studies suggest that people who eat more vegetables and
fruits, which are rich sources of antioxidants (including
vitamin C, vitamin E, carotenoids, and many other antioxidant phytochemicals), may have a lower risk of some
types of cancer.296 Because cancer survivors are at an
increased risk of second cancers,45 they should be encouraged to consume a variety of these antioxidant-rich foods
each day. However, clinical studies of antioxidant dietary
supplements have not demonstrated a reduction in cancer
incidence.297,298 The best advice presently is to obtain
antioxidants through food or beverage sources rather than
dietary supplements.
Is It Safe to Take Antioxidant Supplements
During Cancer Treatment?
Many dietary supplements contain levels of antioxidants
(such as vitamins C and E) that substantially exceed the
amount recommended in the Dietary Reference Intakes
for optimal health.17,21,299 At the present time, evidence is
limited, but taking high doses of supplements with antioxidant activity during chemotherapy or radiation therapy may
be unwise because antioxidants could potentially repair the
cellular oxidative damage to cancer cells that contributes
to the effectiveness of these treatments.300,301 Others,
however, have noted that the possible harm from antioxidants is only hypothetical and that there may be a net
benefit to help protect normal cells from the collateral damage associated with these therapies.23 Whether antioxidants
or any other dietary supplements specifically are beneficial or
harmful during chemotherapy or radiation therapy is a question without a clear scientific answer at this time.22,302-304
Fat
Will Eating Less Total Fat, or Less of Certain Types
of Fat, Lower the Risk of Cancer Recurrence or
Improve Survival?
Several studies have been conducted on the relationship
between fat intake and survival after the diagnosis of breast
cancer, with inconsistent results.136 Preliminary results
from a large clinical trial of early stage breast cancer
survivors suggest that low-fat diets may reduce the risk
of recurrence, particularly in women with ER-negative
disease.91 It is important to note that although there is not
conclusive evidence that total fat consumption influences cancer outcomes, diets very high in fat tend to be high in calories
and may contribute to obesity, which in turn is associated
with an increased cancer incidence at several sites, an
increased risk of recurrence, and a reduced likelihood of
survival for many cancer sites (see Obesity).
There is evidence that certain types of fat, such as
saturated fats, may have an effect on increasing cancer
risk.47,48,305 There is little evidence that other types of fat
(omega-3 fatty acids, found primarily in fish and also
walnuts; monounsaturated fatty acids, found in olive and
canola oils; or other polyunsaturated fats) reduce cancer risk.
In one study, saturated fat intake was inversely associated
with prostate cancer-specific survival and in another, monounsaturated fat intake and risk of death from prostate cancer
were inversely associated.129,130 In addition, excess saturated
fat intake is a known risk factor for cardiovascular diseases,
which are a major cause of morbidity and mortality in all
populations, including cancer survivors. Although trans fats
have adverse cardiovascular effects, such as raising blood
cholesterol levels,49,306 their relationship to cancer incidence
or survival has not been observed. Regardless, due to the relationship with increased cardiovascular disease risk, survivors
should consume as few trans fats as possible. Major sources
of trans fats are some margarines, baked goods, and snack
foods that contain partially hydrogenated oils.
Fiber
Can Dietary Fiber Prevent Cancer or Improve
Cancer Survival?
Dietary fiber includes a wide variety of plant carbohydrates
that are not digestible by humans. Specific categories of
fiber are soluble (such as oat bran) or insoluble (such as
VOLUME 62 _ NUMBER 4 _ JULY/AUGUST 2012
263
wheat bran and cellulose). Soluble fiber helps lower the risk
of coronary heart disease by reducing blood cholesterol
levels. Fiber is also associated with improved bowel function.
Good sources of fiber are beans, vegetables, whole grains,
nuts, and fruits. Consumption of these foods is recommended because they contain other nutrients that may help
reduce cancer risk and provide other health benefits, such as
a reduced risk of coronary heart disease.46
Flaxseed
Obesity
Food Safety
Organic Foods
Physical Activity
Should I Exercise During Cancer Treatment
and Recovery?
Evidence strongly suggests not only that exercise is safe and
feasible during cancer treatment, but also that it
can improve physical functioning and various aspects of
quality of life. Moderate exercise has been shown to
improve fatigue, anxiety, and self-esteem as well as cardiovascular fitness, muscle strength, and body composition.
Phytochemicals
What Are Phytochemicals, and Do They Reduce
Cancer Risk?
The term phytochemicals refers to a wide variety of
biologically active compounds in plants. Some have either
antioxidant or hormone-like actions both in plants and in
individuals who eat them.47 Studies examining the effects
of phytochemicals or selected plant foods such as vegetables
or fruits on cancer recurrence or progression are very
limited, and the little evidence that exists is inconsistent or
comes from only a few studies. There is no evidence that
phytochemicals taken as dietary supplements are as beneficial as the vegetables, fruits, beans, and grains from which
they are extracted.
Soy Products
Is Including Soy-Based Foods in the Diet Recommended
for Cancer Survivors?
Soy and soy-derived foods are an excellent source of protein
and, for this reason, a good alternative to meat. Soy contains
several phytochemicals, some of which have weak estrogenic
activity and seem to protect against hormone-dependent
cancers in animal studies. Other compounds in soy foods
have antioxidant properties and may have anticancer activities. There is considerable public and scientific interest in
the role of soy foods in the prevention of cancer in general
and breast cancer in particular, although scientific support
for such a role is inconsistent.313-316
For the breast cancer survivor, current evidence suggests
no adverse effects on recurrence or survival from consuming
soy and soy foods, and there is the potential for these foods
to exert a positive synergistic effect with tamoxifen.208
Sugar
Does Sugar Feed Cancer?
No. Sugar intake has not been shown to directly increase
the risk or progression of cancer. However, sugars (including honey, raw sugar, brown sugar, high-fructose corn
syrup, and molasses) and beverages that are major sources
of these sugars (such as soft drinks and fruit-flavored beverages) add substantial amounts of calories to the diet and
thus can promote weight gain, which adversely affects
cancer outcomes. In addition, most foods and beverages
that are high in added sugar do not contribute many
nutrients to the diet and often replace more nutritious food
choices. Therefore, limiting the consumption of foods and
beverages with added sugar is recommended.
VOLUME 62 _ NUMBER 4 _ JULY/AUGUST 2012
265
Supplements
Would Survivors Benefit From Using Vitamin and
Mineral Supplements?
Survivors are strongly encouraged to obtain their needed
nutrients through foods, as opposed to supplements. While
dietary supplements are indicated in cases of nutrient
deficiency (either that which is confirmed through laboratory testing or through the clinical presence of disease
[eg, osteoporosis or osteopenia]), given the growing
literature on the adverse effects of nutritional intake beyond
normal levels,161,317 a concern exists that supplements may
do more harm than good.
Can Dietary Supplements Lower Cancer Incidence
or the Risk of Recurrence?
There is no evidence at this time that dietary supplements
can reduce the risk of recurrence or improve the likelihood
of survival.
Vegetarian Diets
Do Vegetarian Diets Reduce the Risk of Cancer
Recurrence?
No studies have demonstrated that consuming a vegetarian
diet has any additional benefit for the prevention of cancer
recurrence over an omnivorous diet high in vegetables,
fruits, and whole grains and low in red meats. However,
vegetarian diets can have many healthful characteristics
because they tend to be low in saturated fat and high in
fiber, vitamins, and phytochemicals320 and are consistent
with the ACS guidelines on nutrition and physical activity
for the prevention of cancer.
References
267
268
67. August DA, Huhmann MB; American Society for Parenteral and Enteral Nutrition
(A.S.P.E.N.) Board of Directors. A.S.P.E.N.
clinical guidelines: nutrition support therapy during adult anticancer treatment and
in hematopoietic cell transplantation. JPEN
J Parenter Enteral Nutr. 2009;33:472-500.
68. Mirtallo J, Canada T, Johnson D, et al;
Task Force for the Revision of Safe Practices for Parenteral Nutrition. Safe practices for parenteral nutrition. JPEN J
Parenter Enteral Nutr. 2004;28:S39-S70.
69. American Dietetic Association. Ethical
and legal issues in nutrition, hydration
and feeding. J Am Diet Assoc. 2008;108:
873-882.
70. Lowe SS, Watanabe SM, Courneya KS.
Physical activity as a supportive care intervention in palliative cancer patients: a systematic review. J Support Oncol. 2009;7:
27-34.
71. Beaton R, Pagdin-Friesen W, Robertson C,
Vigar C, Watson H, Harris SR. Effects of
exercise intervention on persons with metastatic cancer: a systematic review. Physiother Can. 2009;61:141-153.
72. Centers for Disease Control and Prevention. Overweight and Obesity. Atlanta,
GA: Centers for Disease Control and Prevention; 2011. http://www.cdc.gov/obesity/.
Accessed March 23, 2012.
73. Norat T, Chan D, Lau R, Vieira R. The
Associations Between Food, Nutrition and
Physical Activity and the Risk of Breast
Cancer. World Cancer Research Fund/
American Institute for Cancer Research
Systematic Literature Review Continuous
Update Project Report. London: World
Cancer Research Fund/American Institute
for Cancer Research; 2008.
74. Norat T, Chan D, Lau R, Aune D, Vieira R.
The Associations Between Food, Nutrition
and Physical Activity and the Risk of Colorectal Cancer. London: World Cancer
Research Fund/American Institute for
Cancer Research; 2010.
75. Aune D, Greenwood DC, Chan DS, et al.
Body mass index, abdominal fatness and
pancreatic cancer risk: a systematic
review and non-linear dose-response
meta-analysis of prospective studies [published online ahead of print October 3,
2011]. Ann Oncol.
76. McTiernan A, Irwin M, Vongruenigen V.
Weight, physical activity, diet, and prognosis in breast and gynecologic cancers.
J Clin Oncol. 2010;28:4074-4080.
77. Wright ME, Chang SC, Schatzkin A, et al.
Prospective study of adiposity and weight
change in relation to prostate cancer incidence and mortality. Cancer. 2007;109:
675-684.
78. Vrieling A, Kampman E. The role of body
mass index, physical activity, and diet in
colorectal cancer recurrence and survival:
a review of the literature. Am J Clin Nutr.
2010;92:471-490.
79. Irwin ML, Mayne ST. Impact of nutrition
and exercise on cancer survival. Cancer J.
2008;14:435-441.
80. Siegel EM, Ulrich CM, Poole EM, Holmes
RS, Jacobsen PB, Shibata D. The effects of
obesity and obesity-related conditions on
colorectal cancer prognosis. Cancer Control. 2010;17:52-57.
81. Efstathiou JA, Bae K, Shipley WU, et al.
Obesity and mortality in men with locally
advanced prostate cancer: analysis of RTOG
85-31. Cancer. 2007;110:2691-2699.
82. Vance V, Mourtzakis M, McCargar L, Hanning R. Weight gain in breast cancer survivors: prevalence, pattern and health
consequences. Obes Rev. 2011;12:282-294.
98. Rock CL, Demark-Wahnefried W. Nutrition and survival after the diagnosis of
breast cancer: a review of the evidence.
J Clin Oncol. 2002;20:3302-3316.
99. Centers for Disease Control and Prevention. Healthy Weightits not a diet, its a
lifestyle! Atlanta, GA: Centers for Disease
Control and Prevention; 2011. http://
www.cdc.gov/healthyweight/losing_weight/
index.html. Accessed February 12, 2012.
269
114. US Department of Health and Human Services. Physical Activity Guidelines for Americans. Washington, DC: US Department of
Health and Human Services; 2008.
115. Courneya K, Karvinen K, Vallance JK.
Exercise motivation and behavior change.
In: Feuerstein M, ed. Handbook of Cancer
Survivorship. New York: Springer Science-Business Media LLC; 2007:113-132.
116. Pinto BM, Ciccolo JT. Physical activity
motivation and cancer survivorship. Recent
Results Cancer Res. 2011;186:367-387.
117. White SM, McAuley E, Estabrooks PA,
Courneya KS. Translating physical activity
interventions for breast cancer survivors
into practice: an evaluation of randomized
controlled trials. Ann Behav Med. 2009;
37:10-19.
118. US Department of Health and Human
Services. Be Active Your Way: A Fact
Sheet for Adults. Washington, DC: US
Department of Health and Human
Services; 2008. http://www.health.gov/
PAGuidelines/factSheetAdults.aspx. Accessed February 21, 2012.
119. Norman SA, Potashnik SL, Galantino ML, De
Michele AM, House L, Localio AR. Modifiable risk factors for breast cancer recurrence:
what can we tell survivors? J Womens
Health (Larchmt). 2007;16:177-190.
120. Kroenke CH, Fung TT, Hu FB, Holmes
MD. Dietary patterns and survival after
breast cancer diagnosis. J Clin Oncol.
2005;23:9295-9303.
121. Kwan ML, Weltzien E, Kushi LH, Castillo
A, Slattery ML, Caan BJ. Dietary patterns
and breast cancer recurrence and survival
among women with early-stage breast
cancer. J Clin Oncol. 2009;27:919-926.
122. Pierce JP, Natarajan L, Caan BJ, et al.
Influence of a diet very high in vegetables,
fruit, and fiber and low in fat on prognosis
following treatment for breast cancer: the
Womens Healthy Eating and Living
(WHEL) randomized trial. JAMA. 2007;
298:289-298.
123. Meyerhardt JA, Niedzwiecki D, Hollis D,
et al. Association of dietary patterns with
cancer recurrence and survival in patients
with stage III colon cancer. JAMA. 2007;
298:754-764.
124. National Research Council. Dietary Reference Intakes for Energy, Carbohydrate,
Fiber, Fat, Fatty Acids, Cholesterol, Protein, and Amino Acids (Macronutrients).
Washington, DC: The National Academies
Press; 2002.
125. McEligot AJ, Largent J, Ziogas A, Peel D,
Anton-Culver H. Dietary fat, fiber, vegetable, and micronutrients are associated
with overall survival in postmenopausal
women diagnosed with breast cancer.
Nutr Cancer. 2006;55:132-140.
126. Beasley JM, Newcomb PA, TrenthamDietz A, et al. Post-diagnosis dietary factors and survival after invasive breast cancer. Breast Cancer Res Treat. 2011;128:
229-236.
127. Goodwin PJ, Ennis M, Pritchard KI, Koo J,
Trudeau ME, Hood N. Diet and breast cancer: evidence that extremes in diet are
associated with poor survival. J Clin
Oncol. 2003;21:2500-2507.
128. Gold EB, Pierce JP, Natarajan L, et al. Dietary pattern influences breast cancer prognosis in women without hot flashes: the
womens healthy eating and living trial.
J Clin Oncol. 2009;27:352-359.
270
162. Bjelakovic G, Nikolova D, Gluud LL, Simonetti RG, Gluud C. Mortality in randomized trials of antioxidant supplements for
primary and secondary prevention: systematic review and meta-analysis. JAMA.
2007;297:842-857.
163. Hewitt M, Greenfield S, Stovall E, eds. From
Cancer Patient to Cancer Survivor: Lost in
Transition. Washington, DC: Committee on
Cancer Survivorship: Improving Care and
Quality of Life, National Cancer Policy
Board, Institute of Medicine, and National
Research Council of the National Academies: The National Academies Press; 2006.
164. Monti DA, Yang J. Complementary medicine in chronic cancer care. Semin Oncol.
2005;32:225-231.
165. Colditz GA, DeJong W, Hunter DJ, Trichopoulos D, Willett WC. Harvard Report on
Cancer Prevention. Vol 1. Causes of
Human Cancer. Cancer Causes Control.
1996;7(suppl):S3-59.
166. Rimm E. Alcohol and cardiovascular disease. Curr Atheroscler Rep. 2000;2:529-535.
167. OKeefe JH, Bybee KA, Lavie CJ. Alcohol
and cardiovascular health: the razor-sharp
double-edged sword. J Am Coll Cardiol.
2007;50:1009-1014.
168. Barrera S, Demark-Wahnefried W. Nutrition during and after cancer therapy. Oncology (Williston Park). 2009;23(2 suppl
Nurse Ed):15-21.
169. Bellizzi KM, Rowland JH, Jeffery DD,
McNeel T. Health behaviors of cancer survivors: examining opportunities for cancer
control intervention. J Clin Oncol. 2005;
23:8884-8893.
170. Smith-Warner SA, Spiegelman D, Yaun
SS, et al. Alcohol and breast cancer in
women: a pooled analysis of cohort studies. JAMA. 1998;279:535-540.
171. Nielsen SF, Nordestgaard BG, Bojesen SE.
Associations between first and second primary cancers: a population-based study.
CMAJ. 2012;184:E57-E69.
172. Fortin A, Wang CS, Vigneault E. Influence
of smoking and alcohol drinking behaviors on treatment outcomes of patients
with squamous cell carcinomas of the
head and neck. Int J Radiat Oncol Biol
Phys. 2009;74:1062-1069.
173. Reding KW, Daling JR, Doody DR,
OBrien CA, Porter PL, Malone KE. Effect
of prediagnostic alcohol consumption on
survival after breast cancer in young
women. Cancer Epidemiol Biomarkers
Prev. 2008;17:1988-1996.
174. Trentham-Dietz A, Newcomb PA, Nichols
HB, Hampton JM. Breast cancer risk factors and second primary malignancies
among women with breast cancer. Breast
Cancer Res Treat. 2007;105:195-207.
175. Flatt SW, Thomson CA, Gold EB, et al.
Low to moderate alcohol intake is not
associated with increased mortality after
breast cancer. Cancer Epidemiol Biomarkers Prev. 2010;19:681-688.
176. Kwan ML, Kushi LH, Weltzien E, et al.
Alcohol consumption and breast cancer
recurrence and survival among women
with early-stage breast cancer: the life after cancer epidemiology study. J Clin
Oncol. 2010;28:4410-4416.
177. Li CI, Daling JR, Porter PL, Tang MT,
Malone KE. Relationship between potentially modifiable lifestyle factors and risk
of second primary contralateral breast
cancer among women diagnosed with
195.
196.
180. Loi S, Milne RL, Friedlander ML, et al. Obesity and outcomes in premenopausal and
postmenopausal breast cancer. Cancer Epidemiol Biomarkers Prev. 2005;14:1686-1691.
197.
198.
199.
184. Healy LA, Ryan AM, Carroll P, et al. Metabolic syndrome, central obesity and insulin resistance are associated with adverse
pathological features in postmenopausal
breast cancer. Clin Oncol (R Coll Radiol).
2010;22:281-288.
200.
185. Caan BJ, Kwan ML, Hartzell G, et al. Prediagnosis body mass index, post-diagnosis
weight change, and prognosis among
women with early stage breast cancer.
Cancer Causes Control. 2008;19:1319-1328.
201.
202.
203.
204.
188. Herman DR, Ganz PA, Petersen L, Greendale GA. Obesity and cardiovascular risk
factors in younger breast cancer survivors:
The Cancer and Menopause Study
(CAMS). Breast Cancer Res Treat. 2005;
93:13-23.
205.
206.
207.
208.
209.
210.
271
211.
212.
213.
214.
215.
216.
217.
218.
219.
220.
221.
222.
223.
224.
225.
226.
272
for cancer prevention in patients with carcinoma of the skin. A randomized controlled trial. Nutritional Prevention of
Cancer Study Group. JAMA. 1996;276:
1957-1963.
260. Zhou W, Heist RS, Liu G, et al. Circulating
25-hydroxyvitamin D levels predict survival in early-stage non-small-cell lung
cancer patients. J Clin Oncol. 2007;25:
479-485.
261. Sun AS, Ostadal O, Ryznar V, et al. Phase
I/II study of stage III and IV non-small cell
lung cancer patients taking a specific dietary supplement. Nutr Cancer. 1999;34:
62-69.
262. Sun AS, Yeh HC, Wang LH, et al. Pilot
study of a specific dietary supplement in
tumor-bearing mice and in stage IIIB and
IV non-small cell lung cancer patients.
Nutr Cancer. 2001;39:85-95.
263. Evans WK, Nixon DW, Daly JM, et al. A
randomized study of oral nutritional support versus ad lib nutritional intake during
chemotherapy for advanced colorectal and
non-small-cell lung cancer. J Clin Oncol.
1987;5:113-124.
264. Ovesen L, Allingstrup L, Hannibal J, Mortensen EL, Hansen OP. Effect of dietary
counseling on food intake, body weight,
response rate, survival, and quality of life
in cancer patients undergoing chemotherapy: a prospective, randomized study.
J Clin Oncol. 1993;11:2043-2049.
265. Ovesen L, Allingstrup L. Different quantities of two commercial liquid diets consumed by weight-losing cancer patients.
JPEN J Parenter Enteral Nutr. 1992;16:
275-278.
266. Kolonel LN, Nomura AM, Cooney RV. Dietary fat and prostate cancer: current status. J Natl Cancer Inst. 1999;91:414-428.
267. Cohen JH, Kristal AR, Stanford JL. Fruit
and vegetable intakes and prostate cancer
risk. J Natl Cancer Inst. 2000;92:61-68.
268. Freedland SJ, Platz EA. Obesity and prostate cancer: making sense out of apparently conflicting data. Epidemiol Rev.
2007;29:88-97.
269. Meyer F, Bairati I, Shadmani R, Fradet Y,
Moore L. Dietary fat and prostate cancer
survival. Cancer Causes Control. 1999;10:
245-251.
270. Heymach JV, Shackleford TJ, Tran HT,
et al. Effect of low-fat diets on plasma levels of NF-jB-regulated inflammatory cytokines and angiogenic factors in men with
prostate cancer. Cancer Prev Res (Phila).
2011;4:1590-1598.
271. Demark-Wahnefried W, Polascik TJ,
George SL, et al. Flaxseed supplementation (not dietary fat restriction) reduces
prostate cancer proliferation rates in men
presurgery. Cancer Epidemiol Biomarkers
Prev. 2008;17:3577-3587.
272. Fang F, Kasperzyk JL, Shui I, et al. Prediagnostic plasma vitamin D metabolites
and mortality among patients with prostate cancer. PLoS One. 2011;6:e18625.
273. Giovannucci E, Liu Y, Stampfer MJ, Willett WC. A prospective study of calcium
intake and incident and fatal prostate cancer. Cancer Epidemiol Biomarkers Prev.
2006;15:203-210.
274. Beer TM, Eilers KM, Garzotto M, Egorin
MJ, Lowe BA, Henner WD. Weekly highdose calcitriol and docetaxel in metastatic
androgen-independent prostate cancer.
J Clin Oncol. 2003;21:123-128.
273
308. Thompson LU, Chen JM, Li T, StrasserWeippl K, Goss PE. Dietary flaxseed alters
tumor biological markers in postmenopausal breast cancer. Clin Cancer Res.
2005;11:3828-3835.
309. Kono S, Hirohata T. Nutrition and stomach cancer. Cancer Causes Control. 1996;7:
41-55.
310. Sandhu MS, White IR, McPherson K. Systematic review of the prospective cohort
studies on meat consumption and colorectal cancer risk: a meta-analytical
approach. Cancer Epidemiol Biomarkers
Prev. 2001;10:439-446.
311. Norat T, Lukanova A, Ferrari P, Riboli E.
Meat consumption and colorectal cancer
risk: dose-response meta-analysis of epidemiological studies. Int J Cancer. 2002;
98:241-256.
312. Lin KY, Hu YT, Chang KJ, Lin HF, Tsauo
JY. Effects of yoga on psychological
health, quality of life, and physical health
of patients with cancer: a meta-analysis
274